HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055569Generated: October 26, 2026
Bicarbonate Ion → 1-[(5-Bromo-2-chloro-phenyl)methyl]-2,3-difluoro-4-methoxy-benzene
https://huagongshe.com/reaction/1055569
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (5-Bromo-2-chloro-phenyl)-(2,3-difluoro-4-methoxy-phenyl)methanone | HCID 89576925 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[(5-Bromo-2-chloro-phenyl)methyl]-2,3-difluoro-4-methoxy-benzene | HCID 86685107 | 25.9% |
Reaction Steps
To a solution of (5-bromo-2-chloro-phenyl)-(2,3-difluoro-4-methoxy-phenyl)methanone 21e (5.42 g, 14.9 mmol) in acetonitrile (100 mL) were added triethyl silicane (4.8 mL, 29.87 mmol) at 15° C., followed by boron trifluoride diethyl ether (7.4 mL, 59.74 mmol). The mixture was warmed up to room temperature and stirred for 15 hours. To the reaction mixture was added ethyl acetate (4 mL). The mixture was adjusted with saturated aqueous bicarbonate to pH 7, and then partitioned. The combined organic layers were dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo and the residue was purified by silica gel chromatography eluted with PE/EtOAc(v/v)=20/1 to give the title compound 21f as pale yellow oil (1.34 g, 25.8%). The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 347.05 [M+H]+; and 1H NMR (400 MHz, CDCl3) δ (ppm): 7.33 (m, 1H), 7.28 (m, 2H), 6.84-6.76 (m, 1H), 6.75-6.62 (m, 1H), 4.05 (s, 2H), 3.91 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394329B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-55bcdf5271da447982560e6e0bcf2973 |
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| Source note | uspto-grants-2016_07 |
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